Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Spoorthi Jagadish"'
Publikováno v:
Epilepsy & Behavior Reports, Vol 25, Iss , Pp 100652- (2024)
Behr syndrome is associated with compound heterozygous dysfunction in OPA1 gene and typically presents with a constellation of visual impairment due to early onset optic atrophy, cerebellar ataxia, peripheral neuropathy, deafness, and gastrointestina
Externí odkaz:
https://doaj.org/article/78b9d9378d2742c094878487005013ee
Publikováno v:
Epilepsy & Behavior Reports, Vol 16, Iss , Pp 100505- (2021)
Manganese is an essential element that is ubiquitously present in our diet and water supply. It is a cofactor for several critical physiological processes. Elevated blood levels of Manganese secondary to SLC30A10 gene mutation presents distinctly wit
Externí odkaz:
https://doaj.org/article/1468a42a35764b1a9ee1596499f7bc8b
Publikováno v:
Sleep Medicine. 78:43-48
Objective Orthostatic intolerance (OI) is a common manifestation of autonomic dysfunction. It is characterized by light-headedness and palpitations in the upright position, with relief when supine. It can affect the quality of life. Other symptoms th
Autor:
Katherine C. Nickels, Eric T. Payne, Spoorthi Jagadish, Lily C. Wong-Kisiel, Elaine C. Wirrell, Susan Eckert
Publikováno v:
Pediatric Neurology. 94:32-37
Background The ketogenic diet is an accepted treatment modality in refractory childhood epilepsy. In this study, we analyzed the efficacy and tolerability of the ketogenic and modified Atkins diets in children with refractory epilepsy of genetic etio
Autor:
Susan Eckert, Lily C. Wong-Kisiel, Elaine C. Wirrell, Spoorthi Jagadish, Eric T. Payne, Katherine C. Nickels
Publikováno v:
Pediatric Neurology. 95:92-93
Publikováno v:
Pediatric Oncall. 11
Autor:
Spoorthi Jagadish, Santosh Palled
Publikováno v:
Pediatric Oncall. 11
Autor:
Spoorthi Jagadish, Tanavi Ghadage
Publikováno v:
Pediatric Oncall. 11